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@Sarah_T 

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Sarah_T

How do you know if its optic neuritis?

Hi I have RRMS but I've never had optic neuritis but since Monday vision has been blurry in my right eye and I've had a weird headache behind my right eye. The kind thats fine if I keep my head still but if I bend down it really hurts. I've been keeping the headache at bay with paracetamol 3 tim...

@dam205 

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dam205

Primary Progressive MS - A touch Lost

Hello all, Well I don't know where to begin!? Guess I should start here. Joined this site nearly 4 years ago just after I was diagnosed. I have had this thing approximately 20 years. Not on any medication, not that there seems to be much, the same as help with this - not much. I suppose when I w...

The cure for MS for me is travel

I start this year my caminho Santiago. I was afraid always thinking and if a can't walk more that 10km. Well it was amazing day by day I whant more :) I share my croundfounding and in there is all the social media. I beg all the community to share my journey, let me show that is possible for all o...

@dmac95 

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dmac95

FAMPYRA

Hi All I am being put forward to try FAMPYRA to see if it helps with my walking. Today my MS Nurse asked me if I was still taking LDN as she wasn't sure if it would be ok with FAMPYRA. Does anybody have experience or know if it will be ok to take both together.

A short story

What is it like to have Multiple Sclerosis? MS is a strange disease. It attacks you, from every angle, but some you cannot imagine. If you walked around in a space suit that gave you general MS symptoms you would miss a lot. Basically if you have MS you really should be living on a space station. T...

@Tiffany_Roberts 

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Tiffany_Roberts

Living with MS and alternative lifestyle

I'm sorry if this isn't allowed, please delete...I'm just trying to find someone who understands what I'm going through who can maybe offer some words of advice. I am a woman who has lived with MS for about 15 years, abs and I have recently become involved in a BDSM relationship. Does anyone else in...

@watsoncraig 

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watsoncraig

Wobble

The next Zoom meeting that we Falkirk MSrs are having is Sunday June 14th at 11am. This is open to all, MSrs, family or carers regardless of where you are. We have no affiliations and just shoot the 💩 with no agenda nor “top table”.All that’s required is that you drop me a message with an mail addr...

@ncm22 

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ncm22

How long have you had ms ??

Hi everyone. I have had relapsing remitting ms since 2010, symptoms since 2007. Main symptom numbness from waist down on movement. I have had numbness for 10 plus years. I also get tremors from waist down, usually controlled by medication. I get other sensory issues. I didn't start medication till...

@dinnerlady 

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dinnerlady

Treatment help

Hi everyone hope all are keeping safe .Just had a letter from the my M.S. Nurse Informing me my Ocrevus Infusion has been rescheduled to July ( original one cancelled due to virus) I was also told I may be more susceptible to the virus and also may be unable to accept a vaccine for the Virus should ...